Browsing by Author Vasen, Hans
Showing results 1 to 14 of 14
| Issue Date | Title | Author(s) |
|---|---|---|
| 31-May-2021 | A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants | Unhjem Wiik, Mariann; Evans, Tiffany Jane; Belhadj, Sami; Bolton, Katherine A.; Dymerska, Dagmara; Jagmohan Changur, Shantie; Capellá, G. (Gabriel); Kurzawski, Grzegorz; Wijnen, Juul T.; Valle, Laura; Vasen, Hans; Lubinski, Jan; Scott, Rodney J.; Talseth-Palmer, Bente A. |
| 28-Jul-2017 | Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database | Møller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Gareth Evans, D.; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Dominguez Valentin, Mev; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Moeslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group |
| 10-Oct-2017 | Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a prospective lynch syndrome database | Seppälä, Toni T.; Pylvänäinen, Kirsi; Evans, D. Gareth; Järvinen, Heikki; Renkonen-Sinisalo, Laura; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paola; Lindblom, Annika; Macrae, Finlay; Blanco, Inlay; Sijmons, Rolf; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; De Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul; Jenkins, Mark A.; Genuardi, Maurizio; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro, Matilde; Morak, Monika; Frayling, Ian M.; Plazzer, John-Paul; Sampson, Julian R.; Capellá, G. (Gabriel); Möslein, Gabriela; Mecklin, Jukka-Pekka; Møller, Pål; Mallorca Group |
| 1-Feb-2021 | Duodenal adenomas and cancer in MUTYH-associated polyposis: an international cohort study | Collaborative Group on Duodenal Polyposis in MAP; Thomas, Laura E.; Hurley, Joanna J.; Alonso Sánchez, Ángel; Aznárez, M. Rosario; Backman, Ann Sofie; Bjork, Jan; Capellá, G. (Gabriel); Clark, Susan K.; Colas, Chrystelle; Dekker, Evelien; Dolwani, Sunil; Ghorbanoghli, Zeinab; Gonn, Mark; González Romero, S.; Hes, Frederik J.; Jundi, Hala; Kelland, Sarah; Latchford, Andrew R.; Leon Brito, Helena; Lynch, Patrick M.; Meuser, Elena; Mork, Maureen E.; Mort, Matthew; Navarro García, Matilde; Nielsen, Maartje; Parc, Yann; Ricci, Maria T.; Saurin, Jean Christophe; van der Tuin, Karin; Vasen, Hans; Vilar, Eduardo; Vinet, Olivier; Vitellaro, Marco; Walton, Sarah Jane; West, Hannah D.; Sampson, Julian R. |
| 2008 | Guidelines for the clinical management of familial adenomatous polyposis (FAP) | Vasen, Hans; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bernstein, Inge; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Engel, Christoph; Frayling, Ian M.; Friedl, W.; Hes, F. J.; Hodgson, Shirley; Järvinen, Heikki; Mecklin, Jukka-Pekka; Møller, Pål; Myrhoi, T.; Nagengast, F. M.; Parc, Yann; Phillips, R.; Clark, Susan K.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul |
| Sep-2017 | Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database | Møller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Evans, D. Gareth; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Möslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group |
| 1-Dec-2019 | Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers | Page, Elizabeth; Bancroft, Elizabeth K.; Brook, Mark N.; Assel, Melissa; Al Battat, Mona Hassan; Thomas, Sarah; Taylor, Natalie; Chamberlain, Anthony; Pope, Jennifer; Ni Raghallaigh, Holly; Evans, D. Gareth; Offman, Judith; Axcrona, Karol; Obeid, Elias; Dudderidge, Tim; Henderson, Alex; Moynihan, Clare; Eeles, Rosalind A.; Saya, Sibel; Gronberg, Henrik; Castro, Elena; Wilson, Penny; Arun, Banu K.; IMPACT Study Collaborators; Eyfjord, Jorunn E.; Dias, Alexander; Aaronson, Neil K.; Ong, Kai Ren; Lilja, Hans; Kiemeney, Lambertus A. L. M.; Ardern Jones, Audrey; Bangma, Chris H.; Schmutzler, Rita K.; Mckinley, Joanne; Dearnaley, David; Eccles, Diana; Cybulski, Cezary; Falconer, Alison; Rennert, Gadi; Maehle, Lovise; Khoo, Vincent; Van Zelst Stams, Wendy; Helfand, Brian T.; Oosterwijk, Jan C.; Lindeman, Geoffrey J.; Lubinski, Jan; Cardoso, Marta; Kote-Jarai, Zsofia; Mitra, Anita; James, Paul; Suri, Mohnish; Ausems, Margreet G. E. M.; Grindedal, Eli Marie; Rosario, Derek J.; Azzabi, Ashraf; Vickers, Andrew; Wokolorczyk, Dominika; Ringelberg, Janneke; Halliday, Dorothy; Mascarenhas, Lyon; Genova, Elena; Side, Lucy; Thomas, Tessy; Adank, Muriel A.; Teixeira, Manuel R.; Van Asperen, Christi; Domchek, Susan; Vasen, Hans; Ahmed, Munaza; Tischkowitz, Marc; Jensen, Thomas Dyrsø; Osther, Palle J. S.; Liljegren, Annelie; Oldenburg, Rogier A.; Huber, Camilla; Lam, Jimmy; Taylor, Louise; Ronlund, Karina; Ramón y Cajal, Teresa; Salinas Masdeu, Mònica; Van Randeraad, Heleen; Feliubadaló i Elorza, Maria Lídia; Rhiem, Kerstin; Gallagher, David; Cook, Jackie; Foulkes, William D.; Powers, Jacquelyn; Buys, Saundra S.; O'toole, Karen; Izatt, Louise; Susman, Rachel; Greenhalgh, Lynn; Carlsson, Stefan; Tripathi, Vishakha; Williams, Rachel; Cooke, Peter; Aprikian, Armen; Walker, Lisa; Davidson, Rosemarie; Longmuir, Mark; Murthy, Vedang; Van Os, Theo A.; Ruijs, Mariëlle W. G.; Chen Shtoyerman, Rakefet; Helderman Van Den Enden, Apollonia T. J. M.; Donaldson, Alan; Rothwell, Jeanette; Andrews, Lesley; Murphy, Declan G.; Zgajnar, Janez; Jobson, Irene; Morton, Catherine; Shackleton, Kylie; Snape, Katie; Hamdy, Freddie C.; McGrath, John J.; Hanson, Helen; Barwell, Julian; Harris, Marion; Taylor, Amy; Kast, Karin; Kirk, Judy; Johannsson, Oskar; Spigelman, Allan; Pachter, Nicholas; Brewer, Carole; Richardson, Kate; Tricker, Karen; Mikropoulos, Christos; Gadea, Neus; Brady, Angela F.; Copakova, Lucia; Stefansdottir, Vigdis; Foster, Christopher; Teo, Soo H.; Nicolai, Nicola; Friedman, Eitan |
| 28-Feb-2019 | Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report | Seppälä, Toni T.; Ahadova, Aysel; Dominguez Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian R.; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvanainen, Kirsi; Renkonen Sinisalo; Lepisto, Anna; Lautrup, Charlotte K.; Lindblom, Annika; Plazzer, John Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior; Aretz, Stefan; Hüneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Della Valle, Adriana; Neffa, Florencia; Gluck, Nathan; De Vos Tot Nederveen Cappel, Wouter H. WH.; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Blanco Guillermo, Ignacio; ten Broeke, Sanne W.; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian M.; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette; Møller, Pål |
| 28-Jun-2021 | No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study | Dominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål |
| 2010 | Peutz-Jeghers syndrome: a systematic review and recommendations for management | Beggs, A. D.; Latchford, A. R.; Vasen, Hans; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Friedl, W.; Møller, Pål; Hes, F. J.; Järvinen, Heikki; Mecklin, Jukka-Pekka; Nagengast, F. M.; Parc, Yann; Phillips, R. K. S.; Hyer, W.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul; Clark, Susan K.; Hodgson, Shirley V. |
| 1-Dec-2020 | Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report. | Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; González, María Laura; Kalfayan, Pablo; Ryan, Neil A. J.; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Auranen, Annika; Hopper, John L.; Ko Win, Aung; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppälä, Toni T.; Møller, Pål |
| 15-Feb-2021 | The 'unnatural' history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance | Ahadova, Aysel; Seppälä, Toni T.; Engel, Christoph; Gallon, Richard; Burn, John; Holinski Feder, Elke; Steinke Lange, Verena; Möslein, Gabriela; Nielsen, Maartje; Ten Broeke, Sanne W.; Laghi, Luigi; Dominguez Valentin, Mev; Capellá, G. (Gabriel); Macrae, Finlay; Scott, Rodney; Hüneburg, Robert; Nattermann, Jacob; Hoffmeister, Michael; Brenner, Hermann; Bläker, Hendrik; von Knebel Doeberitz, Magnus; Sampson, Julian R.; Vasen, Hans; Mecklin, Jukka-Pekka; Møller, Pål; Kloor, Matthias |
| 17-Mar-2021 | Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report | Seppälä, Toni T.; Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans Georg; Tecklenburg, Johanna; Holinski Feder, Elke; Steinke Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John Paul; Pineda Riu, Marta; Navarro García, Matilde; Vida, Joan B.; Kariv, Revital; Rosner, Guy; Piñero, Tamara A.; Pavicic, Walter Hernán; Kalfayan, Pablo; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; De Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Von Knebel Doeberitz, Magnus; Loeffler, Markus; Redler, Silke; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Hopper, John L.; Win, Aung K.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Wadt, Karin A.W.; Mourits, Marian J.E.; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Rokkones, Erik; Evans, D. Gareth; Møller, Pål |
| 8-Feb-2013 | Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles | Gracia Aznarez, Francisco Javier; Fernandez, Victoria; Pita, Guillermo; Peterlongo, Paolo; Dominguez, Orlando; Hoya, Miguel de la; Durán, Mercedes; Osorio, Ana; Moreno, Leticia; González Neira, Anna; Rosa Rosa, Juan Manuel; Sinilnikova, Olga M.; Mazoyer, Sylvie; Hopper, John L.; Lázaro García, Conxi; Southey, Melissa C.; Odefrey, Fabrice; Manoukian, Siranoush; Catucci, Irene; Caldes, Trinidad; Lynch, Henry T.; Hilbers, Florentine S. M.; van Asperen, Christi J.; Vasen, Hans; Goldgar, David E.; Radice, Paolo; Devilee, Peter; Benitez, Javier |